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Effects of a Non Thermal Plasma Treatment Alone or in Combination with Gemcitabine in a MIA PaCa2-luc Orthotopic Pancreatic Carcinoma Model

Laura BrulléCentre de Recherche Biologique (CERB), Baugy, FranceMarc VandammeCentre d’Imagerie du Petit Animal (CIPA) TAAM, UPS44 CNRS, Orléans, FranceDelphine RièsGREMI UMR-7344 CNRS, Université d'Orléans, Orléans, FranceEric MartelÉric RobertGREMI UMR-7344 CNRS, Université d'Orléans, Orléans, FranceStéphanie LerondelCentre d’Imagerie du Petit Animal (CIPA) TAAM, UPS44 CNRS, Orléans, FranceValérie TrichetINSERM, UMR957, Université de Nantes, Faculté de médecine, Nantes, FranceSerge RichardJean‐Michel PouvesleGREMI UMR-7344 CNRS, Université d'Orléans, Orléans, FranceAlain Le PapeCentre d’Etude des Pathologies Respiratoires (CEPR), INSERM UMR1100-EA6305, Université François Rabelais, Tours, France
2012en
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Pancreatic tumors are the gastrointestinal cancer with the worst prognosis in humans and with a survival rate of 5% at 5 years. Nowadays, no chemotherapy has demonstrated efficacy in terms of survival for this cancer. Previous study focused on the development of a new therapy by non thermal plasma showed significant effects on tumor growth for colorectal carcinoma and glioblastoma. To allow targeted treatment, a fibered plasma (Plasma Gun) was developed and its evaluation was performed on an orthotopic mouse model of human pancreatic carcinoma using a MIA PaCa2-luc bioluminescent cell line. The aim of this study was to characterize this pancreatic carcinoma model and to determine the effects of Plasma Gun alone or in combination with gemcitabine. During a 36 days period, quantitative BLI could be used to follow the tumor progression and we demonstrated that plasma gun induced an inhibition of MIA PaCa2-luc cells proliferation in vitro and in vivo and that this effect could be improved by association with gemcitabine possibly thanks to its radiosensitizing properties.

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